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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Rectal tube — 14 UDI-DI variants, MDR (Medirekt partner s.r.o.)

MD Atlas
Medirekt partner s.r.o.

Data from EUDAMED, last updated May 23, 2026

Rectal tube

859422418RECTALTUBEQJ

14 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Medirekt partner s.r.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 859422418RECTALTUBEQJ
Device name: Rectal tube
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 11, 2026

Manufacturer & authorised representative

Manufacturer

Name: Medirekt partner s.r.o.
SRN: CZ-MF-000053703
Country: Czechia
Email: medirektpartner@email.cz

Variants by status

UDI-DI variants

14 UDI-DI variants

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Applied filters

basicUdiUlid01KRB9ZX2101DP5AAV04WC65GR

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

57230208594224180102
57230108594224180096
57410108594224180133
57311308594224180065
57310408594224180041
57231108594224180119
57310208594224180027
57430108594224180140
57330108594224180072
57310308594224180034
57310908594224180058
57310108594224180010
57330208594224180089
57231208594224180126